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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720873Generated: October 27, 2026

Trifluoroacetic acid → Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/720873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 12136744—
SolventDichloromethaneHCID 6344—
ProductPiperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 1202026095.2%

Reaction Steps

4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (3) (0.77 g; 1.61 mmol) is dissolved in methylene chloride (20 mL) at ambient temperature. Trifluoroacetic acid (20 mL) is added in a slow stream, and the solution is stirred for 90 minutes at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is slurried in a mixture of methylene chloride (10 mL) and water (100 mL), then potassium carbonate is added until the slurry is alkaline. The slurry is diluted with water (200 mL) then extracted with methylene chloride (3×100 mL). The organic extracts are dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (0.58 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135483B2
Source datasetuspto-grants-2006_11
ORD IDord-3c0ff9f4f9494d6dbcba48e765a3b1f0
Source noteuspto-grants-2006_11